Invasive fungal infection by Saprochaete capitata in a child with bone marrow aplasia

Julio Maquera-Afaray1,2, Camila Escajadillo-Vergara2, Jeanpiero Chire-Mercado2

  • 1Instituto Nacional de Salud del Niño San Borja, Lima, Perú.

Insights

Saprochaete capitata is a rare, life-threatening fungal infection in immunocompromised patients. Early detection and treatment are crucial for survival in high-risk individuals, particularly after hematopoietic stem cell transplantation.

Area of Science:

  • Mycology
  • Infectious Diseases
  • Hematology

Background:

  • Saprochaete capitata is an emerging opportunistic pathogen causing invasive fungal infections.
  • These infections are particularly dangerous in immunocompromised individuals, often exhibiting antifungal resistance.
  • Hematopoietic stem cell transplantation (HSCT) recipients are at high risk due to profound immunosuppression.

Observation:

  • A 5-year-old boy with bone marrow aplasia post-HSCT developed persistent febrile neutropenia.
  • Clinical manifestations included abdominal pain, maculopapular skin lesions, and impaired renal function.
  • Saprochaete capitata was identified via blood culture from a central venous catheter.

Findings:

  • The case highlights a rare but severe invasive fungal infection caused by S. capitata.
  • Persistent febrile neutropenia and central venous catheter use were key indicators.
  • The infection presented with multi-organ involvement, including skin and kidneys.

Implications:

  • This case underscores the need for heightened clinical suspicion for S. capitata in febrile neutropenic HSCT patients.
  • Prompt diagnosis and targeted antifungal therapy are critical for improving outcomes.
  • Awareness of this pathogen's potential is vital for managing invasive fungal infections in vulnerable populations.